Llwytho...

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Burdon, K, Wirth, M, Mackey, D, Russell-Eggitt, I, Craig, J, Elder, J, Dickinson, J, Sale, M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Group 2004
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735867/
https://ncbi.nlm.nih.gov/pubmed/15286166
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.018333
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